QMS ++

Make quality part of the workflow.

Connect reviews, evidence and quality records to the laboratory work they govern.

See QMS ++ in action

What “++” means

“++” is the familiar category enhanced by the connected infrastructure behind the broader Scispot lab operating system.

Explore Scispot native apps
  • Keep approvals and evidence in context
  • Support controlled quality workflows
  • Link quality records to operational data

Document Control

  • Centralize and securely manage critical documents, including SOPs, protocols, procedures, and compliance records.
  • Smart automated version control, intuitive approval workflows, and user-friendly acknowledgment tracking.
  • AI-driven reminders ensure proactive compliance.
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Training Management

  • Link staff training directly to relevant documents and SOPs.
  • Automatically monitor real-time training statuses with AI-assisted alerts for upcoming or overdue sessions.
  • Ensure compliance effortlessly with intuitive management dashboards.
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Change Control

  • Highly configurable, no-code workflows for managing changes across lab processes and operations.
  • Detailed tracking, smart reminders, and reporting for every change initiative.
  • Transparent, adaptable, and simple workflows built for evolving lab needs.
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Audit Trails & E-signatures

  • Comprehensive audit logs capturing every action with timestamps and full traceability.
  • Secure electronic signatures that fully comply with regulatory standards, including FDA 21 CFR Part 11.
  • Simplified demonstration of data integrity and regulatory compliance during audits.
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Regulatory Compliance Support

  • Specifically engineered as the best QMS software for pharmaceutical industry standards and life sciences compliance, including GxP, FDA 21 CFR Part 11, ISO 17025, CLIA, and more.
  • Proactive compliance guidance with built-in regulatory checklists.
  • Accelerate audit preparedness with automated compliance tracking.
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Why Scispot QMS ++?

Scispot QMS ++ can be seamlessly bundled with Scispot’s other powerful applications—such as LIMS ++, ELN ++, and GLUE—to create a fully integrated Lab Operating System (LabOS) tailored for comprehensive lab management.

Unified Platform:

Seamlessly integrate quality management with daily lab operations.

Enhanced Efficiency

AI-driven automation reduces manual tasks, errors, and administrative overhead.

Advanced Compliance

Proactive, intelligent features surpassing traditional compliance systems.

White Glove Support

Personalized setups and unlimited expert training and consulting

Connect with 100+ Integrations

Effortlessly integrates via API-first architecture with your existing lab instruments, software, and operational workflows, ensuring comprehensive quality management without disruption.

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Make quality part of the workflow.

Connect reviews, evidence and quality records with Scispot QMS ++.

See QMS ++ in action

QMS ++ FAQs

What exactly is a life sciences QMS, and why do labs need one?

A life sciences QMS is a Quality Management System built specifically for biotech, pharma, diagnostics, and other regulated lab environments. It simplifies managing procedures, documents, and training while ensuring compliance with regulations like FDA, ISO, and GMP. Modern QMS platforms like Scispot QMS ++ reduce manual workload, prevent compliance risks, and enable your team to focus more on science and less on paperwork.

How do we choose the best QMS software for the pharmaceutical industry?

The best QMS software for pharmaceutical industry labs prioritizes compliance, flexibility, and ease of use. Look for systems offering simple document control, robust training management, comprehensive audit trails, and smooth change management. Scispot QMS ++ excels by combining these core capabilities with advanced automation, intuitive workflows, and built-in regulatory checklists designed specifically for pharmaceutical compliance.

How can QMS software for biotech industry labs improve our operational efficiency?

QMS software for biotech industry helps labs manage quality effectively without interrupting research and development. For instance, platforms like Scispot QMS ++ offer configurable, no-code change management and automated training reminders, drastically cutting time spent on manual administrative tasks. Labs gain more time for innovation while effortlessly maintaining compliance and high-quality standards.

Can we integrate a biotech QMS easily with our existing lab instruments and software?

Yes. A modern biotech QMS like Scispot QMS ++ uses an API-first architecture, allowing seamless integration with lab instruments, existing ELNs, LIMS, and other software tools. This integration ensures your quality data is automatically linked to lab workflows, eliminating manual data entry and reducing errors, all while maintaining regulatory compliance.

What makes Scispot QMS ++ stand out compared to traditional QMS for life sciences?

Traditional QMS for life sciences often feels rigid, complex, and difficult to customize. Scispot QMS ++ differs significantly—it’s user-friendly, flexible, and built with intuitive interfaces and powerful automation. This modern approach allows easy adaptation to changing lab processes, proactive compliance management, and significantly less administrative overhead, making it an ideal life sciences QMS choice for forward-thinking lab-based companies.